Evidence map›Paper›PMID 39179924›Full record

ArticleReproductive sciences (Thousand Oaks, Calif.)2024

A Novel Stem Cell Model to Study Preeclampsia Endothelial Dysfunction.

Yanming Wu, Tianyanxin Sun, Pedro Medina, Purnima Narasimhan, David K Stevenson, Frauke Von Versen-Höynck, Jennifer Armstrong, Joseph C Wu, Nazish Sayed, Virginia D Winn

Abstract read
In one paragraph

Article in Reproductive sciences (Thousand Oaks, Calif.), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Yanming WuDepartment of Obstetrics and Gynecology, Stanford University School of Medicine, Stanford, CA, USA.
Tianyanxin SunDepartment of Obstetrics and Gynecology, Stanford University School of Medicine, Stanford, CA, USA.
Pedro MedinaStanford Cardiovascular Institute, Stanford University School of Medicine, Stanford, CA, USA.
Purnima NarasimhanDepartment of Obstetrics and Gynecology, Stanford University School of Medicine, Stanford, CA, USA.
David K StevensonDepartment of Pediatrics, Division of Neonatal and Developmental Medicine, Stanford University School of Medicine, Stanford, CA, USA.
Frauke Von Versen-HöynckDepartment of Obstetrics, Gynecology and Reproductive Sciences, Hannover Medical School, Hannover, Germany.
Jennifer ArmstrongDepartment of Pediatrics, Section of Neurology and Department of Obstetrics and Gynecology, Division of Basic Reproductive Sciences, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Joseph C WuStanford Cardiovascular Institute, Stanford University School of Medicine, Stanford, CA, USA.
Nazish SayedStanford Cardiovascular Institute, Stanford University School of Medicine, Stanford, CA, USA.
Virginia D WinnDepartment of Obstetrics and Gynecology, Stanford University School of Medicine, Stanford, CA, USA. vwinn@stanford.edu.ORCID 0000-0003-1136-2907

Funding

Colorado Clinical and Translational Sciences InstituteUL1TR001082 · NCATS · UNIVERSITY OF COLORADO DENVER · PI SOKOL, RONALD J. · 2013 to 2017
$48.0M
Spectrum Stanford Center for clinical and Translational Research and EducationUL1TR001085 · NCATS · STANFORD UNIVERSITY · PI CULLEN, MARK RICHARD, GREENBERG, HARRY BERNARD · 2013 to 2017
$37.1M
Preeclampsia to cardiovascular disease: Life course analysis of biomarkers and riskR01HL139844 · NHLBI · STANFORD UNIVERSITY · PI HLATKY, MARK A., WINN, VIRGINIA D · 2018 to 2021
$9.0M
UCHSC: Building Interdisciplinary Research Careers in Women's HealthK12HD057022 · NICHD · UNIVERSITY OF COLORADO DENVER · PI REGENSTEINER, JUDITH G., SANTORO, NANETTE F. · 2007 to 2023
$8.5M
BIOREPOSITORY OF HUMAN INDUCED PLURIPOTENT STEM CELLSFORCARDIOVASCULAR DISEASES (BHIPSC-CVD) - TASK AREA B75N92020D00019 · NHLBI · STANFORD UNIVERSITY · PI WU, JOSEPH · 2021 to 2024
$4.0M
Deciphering the Endothelial Cell-Cardiomyocyte Crosstalk in LMNA CardiomyopathyR01HL158641 · NHLBI · STANFORD UNIVERSITY · PI SAYED, NAZISH · 2021 to 2025
$2.2M
Unraveling the role of endothelium in chemotherapy-induced cardiotoxicityR01HL161002 · NHLBI · STANFORD UNIVERSITY · PI SAYED, NAZISH · 2022 to 2025
$1.6M
Functional significance of Siglec-6, a novel leptin receptor, in human placentalR01HD060723 · NICHD · UNIVERSITY OF COLORADO DENVER · PI WINN, VIRGINIA D · 2010 to 2014
$1.5M
American Heart Association South West Affiliates Clinical Research Grant 10CRP3670014German Research Foundation VE490/8-1NCATS NIH HHS UL1 TR001082NCATS NIH HHS UL1 TR001085NHLBI NIH HHS 75N92020D00019NHLBI NIH HHS R01 HL139844NHLBI NIH HHS R01 HL158641NHLBI NIH HHS R01 HL161002NICHD NIH HHS K12 HD057022NICHD NIH HHS R01 HD060723NIH Building Interdisciplinary Research Careers in Women's Health (BIRCWH) K12 HDO57022
6 · The paper itself

Abstract

Preeclampsia is a common pregnancy complication affecting 5% to 7% of all pregnancies worldwide annually. While the pathogenesis is not fully understood, maternal endothelium dysfunction is thought to be a central component to preeclampsia development. Studies to dissect maternal endothelial dysfunction, particularly on a patient-specific basis, are hampered by limited access to systemic primary endothelial cells (ECs). The objective of this study was to establish a replenishable, patient-specific in vitro EC model to allow robust mechanistic studies to dissect endothelial dysfunction in preeclampsia. Induced pluripotent stem cells (iPSCs) from three women with a history of normotensive pregnancies were differentiated into ECs. The established ECs were exposed to pooled sera from normotensive pregnancies, preeclamptic pregnancies, normotensive postpartum for non-pregnant comparison and controls. Endothelial functions including nitric oxide (NO) release, cell migration, tube formation and viability were evaluated. Levels of NO release were significantly lower after incubation with preeclamptic sera compared to the fetal bovine serum (FBS) control, and normotensive and non-pregnant (postpartum) sera treatments were also lower than FBS but higher than preeclamptic sera treatments. Tube formation and cell migration were also impaired with preeclamptic sera compared to FBS controls. Cell viabilities remained unaffected by any sera treatment. Consistent outcomes were obtained across all three patient-specific lines treated with the same pooled sera. Establishment of patient-derived iPSC-ECs treated with pregnancy sera serves as a novel model to explore the interplay between individual maternal endothelial health and circulating factors that lead to endothelial dysfunction in preeclampsia.

Indexed as

Endothelial CellsInduced Pluripotent Stem CellsPre-EclampsiaAdultCell DifferentiationCell MovementCells, CulturedEndothelium, VascularFemaleHumansNitric OxidePregnancyNitric OxideEndothelial dysfunctionHypertensionInduced pluripotent stem cells (iPSCs)PreeclampsiaPregnancy

Identifiers

PMID39179924
PMCPMC11438721

What Socratic holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.